3-168861466-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861466
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861466
    reference: chr 3
allele count: 1
allele frequency: 8.614748449345278e-6
allele num: 116080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-55+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-55+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-55+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-55+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-55+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-55+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-55+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-55+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.510+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-180+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-55+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.138+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-55+20T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10570
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2963
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9999
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1812
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

3-168861475-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861475
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861475
    reference: chr 3
allele count: 1
allele frequency: 8.565603960735272e-6
allele num: 116746
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-55+11A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-55+11A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-55+11A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-55+11A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-180+11A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.510+11A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-55+11A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-55+11A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-55+11A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-55+11A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-55+11A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.138+11A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-55+11A>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2967
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10137
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

3-168861482-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861482
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861482
    reference: chr 3
allele count: 1
allele frequency: 8.504413790757403e-6
allele num: 117586
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-180+4T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-55+4T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-55+4T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-55+4T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-55+4T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.138+4T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-55+4T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-55+4T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-55+4T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-55+4T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-55+4T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-55+4T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.510+4T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7344
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13017
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1813
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.138+4T>C
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: QD

3-168861498-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861498
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861498
    reference: chr 3
allele count: 1
allele frequency: 8.38321345338095e-6
allele num: 119286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.498G>A
  hgvsp: ENST00000494292.1:c.498G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-67G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-67G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-67G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-67G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-67G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-67G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.126G>A
  hgvsp: ENST00000264674.3:c.126G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-67G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-67G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-192G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-67G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-67G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11402
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14224
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln42Gln
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

3-168861499-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861499
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861499
    reference: chr 3
allele count: 1
allele frequency: 8.3760511944249e-6
allele num: 119388
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.125A>G
  hgvsp: ENSP00000264674.3:p.Gln42Arg
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-68A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-68A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-68A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-68A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-68A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-193A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-68A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.497A>G
  hgvsp: ENSP00000417899.1:p.Gln166Arg
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-68A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-68A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-68A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-68A>G
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1815
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14275
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1240
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4684
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln42Arg
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

3-168861501-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861501
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861501
    reference: chr 3
allele count: 3
allele frequency: 2.510754398004787e-5
allele num: 119486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.495C>T
  hgvsp: ENST00000494292.1:c.495C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-70C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-70C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-70C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-70C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.123C>T
  hgvsp: ENST00000264674.3:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-70C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-70C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-70C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-70C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-70C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-70C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-195C>T
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 755
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7385
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1816
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys41Cys
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

3-168861526-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861526
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861526
    reference: chr 3
allele count: 1
allele frequency: 8.304406317992327e-6
allele num: 120418
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.470A>G
  hgvsp: ENSP00000417899.1:p.Tyr157Cys
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-95A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-95A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-95A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.98A>G
  hgvsp: ENSP00000264674.3:p.Tyr33Cys
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-95A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-220A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-95A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-95A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-95A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-95A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-95A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-95A>G
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14572
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1817
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2981
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr33Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-168861536-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861536
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861536
    reference: chr 3
allele count: 561
allele frequency: 4.653979525808432e-3
allele num: 120542
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-105G>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-105G>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-105G>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-105G>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-105G>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-105G>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-230G>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-105G>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-105G>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-105G>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.460G>T
  hgvsp: ENSP00000417899.1:p.Ala154Ser
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.88G>T
  hgvsp: ENSP00000264674.3:p.Ala30Ser
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-105G>T
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7392
  bin: 3.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 4.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 9.75e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 4.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 5.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 10400
  bin: 3.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 11781
  bin: 2.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.75e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 8.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14383
  bin: 2.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 6.75e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.75e1
  variant carriers: 28
genotype quality: GenotypeQuality
hgvs: p.Ala30Ser
num of homozygotes: 2
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD

3-168861536-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861536
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861536
    reference: chr 3
allele count: 1
allele frequency: 8.295863682367972e-6
allele num: 120542
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-105G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.460G>A
  hgvsp: ENSP00000417899.1:p.Ala154Thr
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-105G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-230G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-105G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-105G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-105G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.88G>A
  hgvsp: ENSP00000264674.3:p.Ala30Thr
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-105G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-105G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-105G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-105G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-105G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2989
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4706
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1857
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11781
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14383
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala30Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

3-168861537-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861537
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861537
    reference: chr 3
allele count: 5
allele frequency: 4.147794203042821e-5
allele num: 120546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-106C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-106C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.87C>T
  hgvsp: ENST00000264674.3:c.87C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-231C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-106C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-106C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-106C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.459C>T
  hgvsp: ENST00000494292.1:c.459C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-106C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-106C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-106C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-106C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-106C>T
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4681
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe29Phe
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

3-168861537-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861537
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861537
    reference: chr 3
allele count: 85
allele frequency: 7.051250145172798e-4
allele num: 120546
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-106C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-106C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-106C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-106C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-106C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-106C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.87C>A
  hgvsp: ENSP00000264674.3:p.Phe29Leu
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.459C>A
  hgvsp: ENSP00000417899.1:p.Phe153Leu
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-106C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-106C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-231C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-106C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-106C>A
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4681
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 11854
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 8.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 7360
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1594
  bin: 9.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 14393
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe29Leu
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-168861565-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861565
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861565
    reference: chr 3
allele count: 1
allele frequency: 8.292011476143882e-6
allele num: 120598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-134T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-134T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.431T>G
  hgvsp: ENSP00000417899.1:p.Val144Gly
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.59T>G
  hgvsp: ENSP00000264674.3:p.Val20Gly
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-134T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-134T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-134T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-134T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-259T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-134T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-134T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-134T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-134T>G
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val20Gly
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD

3-168861568-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861568
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861568
    reference: chr 3
allele count: 1
allele frequency: 8.293386853323161e-6
allele num: 120578
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-137A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-137A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.56A>G
  hgvsp: ENSP00000264674.3:p.Asp19Gly
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-137A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-137A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-137A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.428A>G
  hgvsp: ENSP00000417899.1:p.Asp143Gly
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-137A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-137A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-137A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-262A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-137A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-137A>G
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10391
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11924
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp19Gly
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

3-168861569-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861569
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861569
    reference: chr 3
allele count: 7
allele frequency: 5.805178218971322e-5
allele num: 120582
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-138G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-138G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-138G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-263G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-138G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-138G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-138G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-138G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.55G>A
  hgvsp: ENSP00000264674.3:p.Asp19Asn
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.427G>A
  hgvsp: ENSP00000417899.1:p.Asp143Asn
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-138G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-138G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-138G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10390
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1598
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp19Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

3-168861570-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861570
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861570
    reference: chr 3
allele count: 1
allele frequency: 8.292836647703714e-6
allele num: 120586
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-139A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-264A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.54A>C
  hgvsp: ENST00000264674.3:c.54A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-139A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-139A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-139A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-139A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-139A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.426A>C
  hgvsp: ENST00000494292.1:c.426A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-139A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-139A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-139A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-139A>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14354
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11922
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1599
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro18Pro
num of homozygotes: 0
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

3-168861572-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861572
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861572
    reference: chr 3
allele count: 6
allele frequency: 4.975701988622228e-5
allele num: 120586
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-141C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-266C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-141C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-141C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-141C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-141C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-141C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.424C>T
  hgvsp: ENSP00000417899.1:p.Pro142Ser
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.52C>T
  hgvsp: ENSP00000264674.3:p.Pro18Ser
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-141C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-141C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-141C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-141C>T
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11927
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1600
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro18Ser
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

3-168861582-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861582
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861582
    reference: chr 3
allele count: 1
allele frequency: 8.296138976920141e-6
allele num: 120538
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.414T>C
  hgvsp: ENST00000494292.1:c.414T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-151T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-151T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-151T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-151T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-151T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-276T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-151T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.42T>C
  hgvsp: ENST00000264674.3:c.42T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-151T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-151T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-151T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-151T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp14Asp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

3-168861583-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861583
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861583
    reference: chr 3
allele count: 1
allele frequency: 8.296276631047985e-6
allele num: 120536
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.413A>G
  hgvsp: ENSP00000417899.1:p.Asp138Gly
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-152A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-152A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-152A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-152A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-152A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-152A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-152A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.41A>G
  hgvsp: ENSP00000264674.3:p.Asp14Gly
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-152A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-152A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-152A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-277A>G
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10398
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp14Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

3-168861588-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861588
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861588
    reference: chr 3
allele count: 1
allele frequency: 8.299719469481931e-6
allele num: 120486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-157C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-157C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-157C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-157C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.408C>T
  hgvsp: ENST00000494292.1:c.408C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-157C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-157C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-157C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.36C>T
  hgvsp: ENST00000264674.3:c.36C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-157C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-157C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-282C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-157C>T
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14183
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys12Cys
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

3-168861591-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861591
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861591
    reference: chr 3
allele count: 3
allele frequency: 2.490701381509033e-5
allele num: 120448
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.33C>A
  hgvsp: ENSP00000264674.3:p.Phe11Leu
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-160C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-160C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-160C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-160C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-160C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-160C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-160C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-160C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.405C>A
  hgvsp: ENSP00000417899.1:p.Phe135Leu
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-160C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-160C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-285C>A
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10392
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe11Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

3-168861597-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861597
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861597
    reference: chr 3
allele count: 1
allele frequency: 8.309512730173502e-6
allele num: 120344
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.27G>A
  hgvsp: ENST00000264674.3:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-166G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-166G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-166G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-166G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-166G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-291G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-166G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-166G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.399G>A
  hgvsp: ENST00000494292.1:c.399G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-166G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-166G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-166G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4687
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1603
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val9Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD

3-168861607-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861607
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861607
    reference: chr 3
allele count: 1
allele frequency: 8.334583520861462e-6
allele num: 119982
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.389T>C
  hgvsp: ENSP00000417899.1:p.Phe130Ser
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-301T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-176T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-176T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-176T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-176T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-176T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-176T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-176T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-176T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.17T>C
  hgvsp: ENSP00000264674.3:p.Phe6Ser
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-176T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-176T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe6Ser
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD

3-168861608-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861608
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861608
    reference: chr 3
allele count: 1
allele frequency: 8.335139280177371e-6
allele num: 119974
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-177T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-177T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-177T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-177T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-177T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-177T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.388T>A
  hgvsp: ENSP00000417899.1:p.Phe130Ile
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.16T>A
  hgvsp: ENSP00000264674.3:p.Phe6Ile
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-177T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-177T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-177T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-177T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-302T>A
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13461
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1605
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4682
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7357
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe6Ile
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

3-168861611-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861611
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861611
    reference: chr 3
allele count: 1
allele frequency: 8.347245409015026e-6
allele num: 119800
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-305G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-180G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-180G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-180G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.13G>A
  hgvsp: ENSP00000264674.3:p.Glu5Lys
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-180G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.385G>A
  hgvsp: ENSP00000417899.1:p.Glu129Lys
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-180G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-180G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-180G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-180G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-180G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-180G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11763
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu5Lys
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

3-168861612-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861612
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861612
    reference: chr 3
allele count: 405
allele frequency: 3.380295796748239e-3
allele num: 119812
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-181C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-181C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.384C>T
  hgvsp: ENST00000494292.1:c.384C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-181C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-181C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-181C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-181C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-181C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-181C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.12C>T
  hgvsp: ENST00000264674.3:c.12C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-181C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-306C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-181C>T
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1969
  bin: 9.75e1
  variant carriers: 366
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4656
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11689
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 13162
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp4Asp
num of homozygotes: 9
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

3-168861613-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861613
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861613
    reference: chr 3
allele count: 3
allele frequency: 2.504549932377152e-5
allele num: 119782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-182A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-182A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-182A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.11A>G
  hgvsp: ENSP00000264674.3:p.Asp4Gly
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-182A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-182A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-182A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-307A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-182A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-182A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.383A>G
  hgvsp: ENSP00000417899.1:p.Asp128Gly
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-182A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-182A>G
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 841
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10253
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7299
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp4Gly
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

3-168861625-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861625
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861625
    reference: chr 3
allele count: 1
allele frequency: 8.389543273264204e-6
allele num: 119196
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-5T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-5T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-5T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-5T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-5T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-189-5T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-189-5T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-189-5T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.4-5T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-5T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-189-5T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-5T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-5T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10194
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12206
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.4-5T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff

3-168861627-GGAA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861627
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861624
    reference: chr 3
allele count: 1
allele frequency: 8.397997917296517e-6
allele num: 119076
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-189-10_-189-8delTTC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-10_-314-8delTTC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-10_-189-8delTTC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-10_-189-8delTTC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-10_376-8delTTC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-189-10_-189-8delTTC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.4-10_4-8delTTC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-189-10_-189-8delTTC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-10_-189-8delTTC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-189-10_-189-8delTTC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-10_-189-8delTTC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-10_-189-8delTTC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-10_-189-8delTTC
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.4-10_4-8delTTC
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: GGAA
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

3-168861629-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861629
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861629
    reference: chr 3
allele count: 3
allele frequency: 2.520203632453502e-5
allele num: 119038
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-9T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-189-9T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-189-9T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-9T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-189-9T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-9T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-9T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-9T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-9T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-9T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-9T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-189-9T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.4-9T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11965
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11205
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-168861630-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861630
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861630
    reference: chr 3
allele count: 1
allele frequency: 8.406328283932143e-6
allele num: 118958
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-10T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-10T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-189-10T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-189-10T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-10T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-189-10T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-10T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-10T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-189-10T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-10T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-10T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-10T>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.4-10T>A
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11125
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10171
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7295
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11782
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

3-168861643-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861643
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861643
    reference: chr 3
allele count: 2
allele frequency: 1.686369078736572e-5
allele num: 118598
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-189-23T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-189-23T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-23T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-23T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-189-23T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-23T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-23T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.4-23T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-23T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-189-23T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-23T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-23T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-23T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10832
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10145
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

3-168861656-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861656
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861655
    reference: chr 3
allele count: 4
allele frequency: 3.389485815001864e-5
allele num: 118012
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-37delA
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.4-37delA
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-37delA
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-37delA
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-189-37delA
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-189-37delA
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-189-37delA
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-37delA
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-37delA
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-37delA
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-37delA
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-189-37delA
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-37delA
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2753
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10375
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 998
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: AT
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

3-168861658-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861658
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861658
    reference: chr 3
allele count: 3
allele frequency: 2.545220076695965e-5
allele num: 117868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-38A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.4-38A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-38A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-38A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-189-38A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-189-38A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-38A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-38A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-189-38A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-189-38A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-38A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-38A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-38A>G
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1875
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10481
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2734
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10307
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

3-168861661-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861661
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861661
    reference: chr 3
allele count: 5
allele frequency: 4.25684074307412e-5
allele num: 117458
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-41G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-189-41G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-41G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-41G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-41G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-189-41G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-41G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-189-41G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-41G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-41G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-41G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-189-41G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.4-41G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7278
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1685
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10254
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-168861666-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168861666
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168861666
    reference: chr 3
allele count: 1
allele frequency: 8.530676312018017e-6
allele num: 117224
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-189-46A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-46A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-189-46A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-46A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-46A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-189-46A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-189-46A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-46A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-46A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-46A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-46A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-46A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.4-46A>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 999
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10345
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum

3-168862751-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168862751
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168862751
    reference: chr 3
allele count: 2
allele frequency: 7.210325185665874e-5
allele num: 27738
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-1131T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-1131T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-1131T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-190+34T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-1131T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-190+34T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-190+34T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-190+34T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-1131T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-1131T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-1131T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-1131T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.3+34T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22373
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21953
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1333
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

3-168862760-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168862760
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168862760
    reference: chr 3
allele count: 1
allele frequency: 3.473910928923782e-5
allele num: 28786
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-1140A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-190+25A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-1140A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-1140A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-1140A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-1140A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-1140A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-190+25A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-1140A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-190+25A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-190+25A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.3+25A>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-1140A>G
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20389
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22347
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

3-168862760-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168862760
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168862760
    reference: chr 3
allele count: 3847
allele frequency: 1.336413534356979e-1
allele num: 28786
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-1140A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-1140A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-190+25A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-1140A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-1140A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-1140A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-190+25A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-190+25A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-1140A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-1140A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-190+25A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.3+25A>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-1140A>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 2.75e1
  variant carriers: 142
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 4.75e1
  variant carriers: 238
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 5.25e1
  variant carriers: 215
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 9.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 1.25e1
  variant carriers: 1118
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 1.75e1
  variant carriers: 278
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.25e1
  variant carriers: 226
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 3.25e1
  variant carriers: 179
genotype depth: GenotypeDepth
  all individuals: 20389
  bin: 2.5e0
  variant carriers: 463
genotype depth: GenotypeDepth
  all individuals: 22347
  bin: 7.5e0
  variant carriers: 2350
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 2.25e1
  variant carriers: 107
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 6.75e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 3.75e1
  variant carriers: 215
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 225
  bin: 6.25e1
  variant carriers: 105
genotype depth: GenotypeDepth
  all individuals: 2487
  bin: 9.75e1
  variant carriers: 447
genotype quality: GenotypeQuality
num of homozygotes: 281
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

3-168862770-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168862770
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168862770
    reference: chr 3
allele count: 1
allele frequency: 3.701510216168196e-5
allele num: 27016
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-1150T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-1150T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-1150T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-190+15T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-1150T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-1150T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-190+15T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-1150T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-190+15T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-1150T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-1150T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-190+15T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.3+15T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21571
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2372
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP

3-168862775-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168862775
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168862775
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 26850
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.3+10T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-190+10T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-1155T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-190+10T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-1155T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-190+10T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-1155T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-190+10T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-1155T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-1155T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-1155T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-1155T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-1155T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 23522
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20971
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3313
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-168862779-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168862779
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168862779
    reference: chr 3
allele count: 1
allele frequency: 3.766478342749529e-5
allele num: 26550
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-190+6T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-1159T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-190+6T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-1159T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-190+6T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-1159T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-1159T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.3+6T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-1159T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-190+6T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-1159T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-1159T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-1159T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24068
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3236
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20454
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3+6T>C
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: A
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-168862802-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168862802
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168862802
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 24782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-207T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-207T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-207T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.-15T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-1182T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-1182T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-207T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-1182T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-1182T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-189-1182T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-1182T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-1182T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-189-1182T>G
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16826
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2721
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27504
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

3-168862832-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168862832
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168862832
    reference: chr 3
allele count: 0
allele frequency: 0.0e0
allele num: 22956
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-314-1212C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419757
  ensembl transcript: ENST00000487503
  gene symbol: MECOM
  hgvsc: ENST00000487503.1:c.-237C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000394302
  ensembl transcript: ENST00000433243
  gene symbol: MECOM
  hgvsc: ENST00000433243.2:c.-237C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-189-1212C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000264674
  ensembl transcript: ENST00000264674
  gene symbol: MECOM
  hgvsc: ENST00000264674.3:c.-45C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-1212C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417922
  ensembl transcript: ENST00000460890
  gene symbol: MECOM
  hgvsc: ENST00000460890.1:c.-237C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-189-1212C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-1212C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420072
  ensembl transcript: ENST00000494597
  gene symbol: MECOM
  hgvsc: ENST00000494597.1:c.-237C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000376493
  ensembl transcript: ENST00000392736
  gene symbol: MECOM
  hgvsc: ENST00000392736.3:c.-190+1182C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-189-1212C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000420048
  ensembl transcript: ENST00000472280
  gene symbol: MECOM
  hgvsc: ENST00000472280.1:c.-190+1182C>T
  variant of: http://identifiers.org/hgnc/3498
canonical: true
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15502
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1231
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28847
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2371
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

3-168864219-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864219
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864219
    reference: chr 3
allele count: 1
allele frequency: 8.917901796065422e-6
allele num: 112134
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-315+46C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-190+46C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-190+65C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2599C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+292C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2599C>G
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15985
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18755
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 815
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7077
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22901
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10056
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 575
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6391
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

3-168864222-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864222
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864222
    reference: chr 3
allele count: 1
allele frequency: 8.915039671926539e-6
allele num: 112170
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2602C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+289C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-190+43C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-190+62C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2602C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-315+43C>G
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3542
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 575
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18811
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16020
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3088
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4396
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1983
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6384
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 23305
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

3-168864225-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864225
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864225
    reference: chr 3
allele count: 1
allele frequency: 8.919333547397339e-6
allele num: 112116
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+286G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2605G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-190+40G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2605G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-315+40G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-190+59G>C
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18905
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5287
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10033
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 538
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23553
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3568
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

3-168864226-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864226
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864226
    reference: chr 3
allele count: 2
allele frequency: 1.783039726125098e-5
allele num: 112168
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2606C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-190+58C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2606C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-190+39C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+285C>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-315+39C>A
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7053
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1895
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23633
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4353
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1460
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10050
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6362
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

3-168864231-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864231
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864231
    reference: chr 3
allele count: 3
allele frequency: 2.673558506371981e-5
allele num: 112210
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-190+34C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-315+34C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+280C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-190+53C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2611C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2611C>G
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3530
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7039
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19130
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 9.25e1
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genotype depth: GenotypeDepth
  all individuals: 5439
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 225
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  variant carriers: 0
genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10078
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genotype quality: GenotypeQuality
  all individuals: 3056
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genotype quality: GenotypeQuality
  all individuals: 24196
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genotype quality: GenotypeQuality
  all individuals: 4338
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD

3-168864244-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864244
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864244
    reference: chr 3
allele count: 1
allele frequency: 8.906781623528155e-6
allele num: 112274
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-190+21G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2624G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-315+21G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+267G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2624G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-190+40G>C
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19326
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5656
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
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  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6357
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4345
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1455
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

3-168864245-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864245
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864245
    reference: chr 3
allele count: 1
allele frequency: 8.902975374370115e-6
allele num: 112322
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2625T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-315+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2625T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-190+39T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-190+20T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+266T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3527
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24826
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 574
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3059
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1456
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4351
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1977
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

3-168864262-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864262
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864262
    reference: chr 3
allele count: 1
allele frequency: 8.894739650970415e-6
allele num: 112426
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-315+3G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-190+22G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-190+3G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2642G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2642G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+249G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3528
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5801
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19473
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3063
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 605
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4354
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6359
  bin: 9.75e1
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genotype quality: GenotypeQuality
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 174
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
hgvs: c.-190+3G>A
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

3-168864271-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864271
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864271
    reference: chr 3
allele count: 3
allele frequency: 2.667520273154076e-5
allele num: 112464
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-196G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+240G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-190+13G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-321G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2651G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2651G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16155
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1889
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3567
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10171
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25092
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1979
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP

3-168864272-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864272
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864272
    reference: chr 3
allele count: 2
allele frequency: 1.778220357066648e-5
allele num: 112472
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-197G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-322G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2652G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-190+12G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2652G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+239G>C
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1457
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3566
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1980
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6360
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

3-168864272-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864272
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864272
    reference: chr 3
allele count: 2
allele frequency: 1.778220357066648e-5
allele num: 112472
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2652G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-322G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-197G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-190+12G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+239G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2652G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16156
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7040
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3526
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1457
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6360
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1980
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 618
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3060
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-168864275-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864275
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864275
    reference: chr 3
allele count: 1188
allele frequency: 1.055962454668278e-2
allele num: 112504
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-325T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+236T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-190+9T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-200T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2655T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2655T>G
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19367
  bin: 2.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 15988
  bin: 3.25e1
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6909
  bin: 3.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 5646
  bin: 2.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.25e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 3439
  bin: 4.25e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 8.25e1
  variant carriers: 54
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 69
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 5.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 4.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 60
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 505
  bin: 5.75e1
  variant carriers: 44
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 9.75e1
  variant carriers: 410
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 47
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 9.25e1
  variant carriers: 63
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 8.75e1
  variant carriers: 66
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2981
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6977
  bin: 9.75e1
  variant carriers: 1098
genotype quality: GenotypeQuality
  all individuals: 24929
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 8.75e1
  variant carriers: 2
num of homozygotes: 79
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP

3-168864292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864292
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864292
    reference: chr 3
allele count: 1
allele frequency: 8.883677131638327e-6
allele num: 112566
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-342G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2672G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-217G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+219G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2672G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-198G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19874
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
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  variant carriers: 0
genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25582
  bin: 6.25e1
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genotype quality: GenotypeQuality
  all individuals: 20
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genotype quality: GenotypeQuality
  all individuals: 1938
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genotype quality: GenotypeQuality
  all individuals: 3029
  bin: 8.25e1
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genotype quality: GenotypeQuality
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  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5947
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
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  bin: 6.75e1
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genotype quality: GenotypeQuality
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  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 609
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 8.75e1
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genotype quality: GenotypeQuality
  all individuals: 1
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum

3-168864295-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864295
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864295
    reference: chr 3
allele count: 2
allele frequency: 1.776672292795594e-5
allele num: 112570
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-345C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2675C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-201C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2675C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-220C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+216C>T
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16306
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5752
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
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  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.25e1
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genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
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genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
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genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1830
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 8.75e1
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genotype quality: GenotypeQuality
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  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 5947
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 125
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 10339
  bin: 6.75e1
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genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
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genotype quality: GenotypeQuality
  all individuals: 621
  bin: 7.5e0
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genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4336
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/3-168864301-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864301
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864301
    reference: chr 3
allele count: 1
allele frequency: 8.88320363856021e-6
allele num: 112572
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-226T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-351T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-207T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+210T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2681T>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2681T>G
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
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genotype depth: GenotypeDepth
  all individuals: 16303
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
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genotype depth: GenotypeDepth
  all individuals: 43
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genotype depth: GenotypeDepth
  all individuals: 19891
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genotype depth: GenotypeDepth
  all individuals: 6970
  bin: 3.75e1
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genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
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genotype depth: GenotypeDepth
  all individuals: 244
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genotype depth: GenotypeDepth
  all individuals: 5756
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genotype depth: GenotypeDepth
  all individuals: 668
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genotype depth: GenotypeDepth
  all individuals: 16
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genotype depth: GenotypeDepth
  all individuals: 36
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genotype depth: GenotypeDepth
  all individuals: 113
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genotype depth: GenotypeDepth
  all individuals: 10
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genotype depth: GenotypeDepth
  all individuals: 29
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genotype depth: GenotypeDepth
  all individuals: 18
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genotype quality: GenotypeQuality
  all individuals: 1417
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 9
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genotype quality: GenotypeQuality
  all individuals: 3029
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 10
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genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
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genotype quality: GenotypeQuality
  all individuals: 14
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genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

3-168864303-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864303
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864303
    reference: chr 3
allele count: 3
allele frequency: 2.664961091568063e-5
allele num: 112572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2683G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-353G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-228G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+208G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-209G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2683G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19891
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
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  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
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genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 2.5e0
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genotype depth: GenotypeDepth
  all individuals: 466
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16305
  bin: 3.25e1
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genotype depth: GenotypeDepth
  all individuals: 245
  bin: 6.25e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 5753
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genotype depth: GenotypeDepth
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  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
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genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 3.75e1
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genotype depth: GenotypeDepth
  all individuals: 1830
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genotype quality: GenotypeQuality
  all individuals: 9
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genotype quality: GenotypeQuality
  all individuals: 1
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genotype quality: GenotypeQuality
  all individuals: 1934
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genotype quality: GenotypeQuality
  all individuals: 5947
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genotype quality: GenotypeQuality
  all individuals: 14
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 4335
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genotype quality: GenotypeQuality
  all individuals: 122
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

3-168864307-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864307
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864307
    reference: chr 3
allele count: 1
allele frequency: 8.883045818750333e-6
allele num: 112574
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-232G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2687G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2687G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-213G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+204G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-357G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6969
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 16307
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genotype depth: GenotypeDepth
  all individuals: 1829
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 244
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 71
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genotype depth: GenotypeDepth
  all individuals: 466
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 650
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3029
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genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

3-168864320-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864320
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864320
    reference: chr 3
allele count: 8
allele frequency: 7.106184156762423e-5
allele num: 112578
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-370C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-245C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+191C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2700C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2700C>G
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-226C>G
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16305
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19896
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6968
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 10349
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5950
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 4331
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1933
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

3-168864321-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864321
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864321
    reference: chr 3
allele count: 1
allele frequency: 8.882572392965002e-6
allele num: 112580
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-227C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-246C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2701C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2701C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+190C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-371C>T
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16308
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5761
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19903
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
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genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25615
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3031
  bin: 8.25e1
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genotype quality: GenotypeQuality
  all individuals: 586
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1933
  bin: 9.25e1
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genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
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genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff

3-168864325-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864325
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864325
    reference: chr 3
allele count: 1
allele frequency: 8.88320363856021e-6
allele num: 112572
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2705T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+186T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-231T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418828
  ensembl transcript: ENST00000475754
  gene symbol: MECOM
  hgvsc: ENST00000475754.1:c.-375T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2705T>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-250T>C
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6967
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5941
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.25e1
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genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
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genotype quality: GenotypeQuality
  all individuals: 579
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
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genotype quality: GenotypeQuality
  all individuals: 1933
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genotype quality: GenotypeQuality
  all individuals: 4332
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ

3-168864336-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864336
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864336
    reference: chr 3
allele count: 1
allele frequency: 8.885413704862098e-6
allele num: 112544
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+175G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-261G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-242G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2716G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2716G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3434
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genotype depth: GenotypeDepth
  all individuals: 91
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5699
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genotype depth: GenotypeDepth
  all individuals: 18
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16300
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
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  variant carriers: 0
genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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genotype depth: GenotypeDepth
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6968
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genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  variant carriers: 0
genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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  bin: 3.75e1
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genotype quality: GenotypeQuality
  all individuals: 546
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genotype quality: GenotypeQuality
  all individuals: 11
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genotype quality: GenotypeQuality
  all individuals: 17
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10340
  bin: 6.75e1
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
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genotype quality: GenotypeQuality
  all individuals: 3
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1933
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genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD

3-168864348-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864348
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864348
    reference: chr 3
allele count: 2
allele frequency: 1.777682968019483e-5
allele num: 112506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2728G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2728G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-273G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-254G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+163G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19869
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3574
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5942
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25431
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10315
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

3-168864348-CGT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864348
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864346
    reference: chr 3
allele count: 8
allele frequency: 7.110731872077934e-5
allele num: 112506
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-275_-274delAC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417299
  ensembl transcript: ENST00000484519
  gene symbol: MECOM
  hgvsc: ENST00000484519.1:c.-256_-255delAC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+161_-190+162delAC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2730_-189-2729delAC
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2730_376-2729delAC
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6963
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5942
  bin: 9.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 25431
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4326
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1414
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10315
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3574
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: CGT
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

3-168864371-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864371
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864371
    reference: chr 3
allele count: 2
allele frequency: 1.783166904422254e-5
allele num: 112160
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2751G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+140G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2751G>C
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-296G>C
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6933
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9931
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3488
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5928
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4266
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2990
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1921
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

3-168864371-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864371
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864371
    reference: chr 3
allele count: 1
allele frequency: 8.91583452211127e-6
allele num: 112160
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+140G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2751G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-296G>A
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2751G>A
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6933
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1826
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4266
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3488
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2990
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1404
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9931
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum

3-168864372-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 168864372
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 168864372
    reference: chr 3
allele count: 1
allele frequency: 8.918060856847287e-6
allele num: 112132
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000417899
  ensembl transcript: ENST00000494292
  gene symbol: MECOM
  hgvsc: ENST00000494292.1:c.376-2752C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419995
  ensembl transcript: ENST00000468789
  gene symbol: MECOM
  hgvsc: ENST00000468789.1:c.-297C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000418046
  ensembl transcript: ENST00000481315
  gene symbol: MECOM
  hgvsc: ENST00000481315.1:c.-189-2752C>T
  variant of: http://identifiers.org/hgnc/3498
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000085276
  ensembl protein: ENSP00000419770
  ensembl transcript: ENST00000464456
  gene symbol: MECOM
  hgvsc: ENST00000464456.1:c.-190+139C>T
  variant of: http://identifiers.org/hgnc/3498
canonical: false
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19297
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 11549
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 434
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7298
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1020
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3479
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2456
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4519
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2278
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
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variant carriers: 0

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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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African
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InbreedingCoeff
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QD
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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MQ
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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African
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East Asian
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South Asian
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European (Non-Finnish)
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Other
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QD
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MQRankSum
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FS
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

African
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East Asian
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European (Non-Finnish)
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Latino
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Other
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South Asian
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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BaseQRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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East Asian
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Latino
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South Asian
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African
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Other
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DP
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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FS
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ReadPosRankSum
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QD
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DP
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BaseQRankSum
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MQ
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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Other
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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East Asian
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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DP
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FS
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MQ
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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European (Finnish)
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African
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Latino
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South Asian
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QD
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DP
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ClippingRankSum
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FS
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VQSLOD
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MQ
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 2

European (Finnish)
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allele count: 2
allele frequency: 3.02571860816944e-4
allele num: 6610
num of homozygotes: 0

African
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allele count: 36
allele frequency: 3.680981595092025e-3
allele num: 9780
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 33
allele frequency: 2.856648199445983e-3
allele num: 11552
num of homozygotes: 0

Other
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allele count: 15
allele frequency: 1.677852348993289e-2
allele num: 894
num of homozygotes: 0

South Asian
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allele count: 261
allele frequency: 1.586047642197375e-2
allele num: 16456
num of homozygotes: 2

European (Non-Finnish)
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allele count: 214
allele frequency: 3.211862880470673e-3
allele num: 66628
num of homozygotes: 0

BaseQRankSum
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SIO_000300: -1.407e0

MQ
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SIO_000300: 5.983e1

DP
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InbreedingCoeff
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SIO_000300: 1.49e-2

ReadPosRankSum
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SIO_000300: 5.98e-1

MQRankSum
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VQSLOD
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ClippingRankSum
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SIO_000300: -1.91e-1

FS
type: SiteQuality
SIO_000300: 6.01e-1

QD
type: SiteQuality
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.01e-1

DP
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MQ
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SIO_000300: 5.983e1

BaseQRankSum
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SIO_000300: -1.407e0

ReadPosRankSum
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SIO_000300: 5.98e-1

InbreedingCoeff
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VQSLOD
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SIO_000300: 4.81e0

MQRankSum
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SIO_000300: 2.93e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.91e-1

QD
type: SiteQuality
SIO_000300: 1.394e1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.003301815998799e-5
allele num: 66630
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.022285831118381e-4
allele num: 9782
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

DP
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SIO_000300: 2.224128e6

QD
type: SiteQuality
SIO_000300: 1.446e1

VQSLOD
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SIO_000300: 4.76e0

BaseQRankSum
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SIO_000300: 3.71e0

FS
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SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 5

GenotypeDepth
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variant carriers: 4

GenotypeDepth
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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 15
allele frequency: 2.26928895612708e-3
allele num: 6610
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
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allele count: 70
allele frequency: 1.05057781779979e-3
allele num: 66630
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
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SIO_000300: 2.224128e6

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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QD
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MQRankSum
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SIO_000300: 2.09e-1

InbreedingCoeff
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BaseQRankSum
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SIO_000300: 3.71e0

MQ
type: SiteQuality
SIO_000300: 5.982e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.75e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele count: 0
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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FS
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MQ
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QD
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VQSLOD
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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QD
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MQ
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ClippingRankSum
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FS
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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DP
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VQSLOD
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 7
allele frequency: 8.118765947575968e-4
allele num: 8622
num of homozygotes: 0

European (Non-Finnish)
type: Population
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.952e1

FS
type: SiteQuality
SIO_000300: 1.203e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

ClippingRankSum
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SIO_000300: -6.24e-1

BaseQRankSum
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SIO_000300: -3.83e0

MQRankSum
type: SiteQuality
SIO_000300: 7.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.51e-1

DP
type: SiteQuality
SIO_000300: 2.224959e6

QD
type: SiteQuality
SIO_000300: 1.262e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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InbreedingCoeff
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DP
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MQRankSum
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VQSLOD
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SIO_000300: 1.92e-1

BaseQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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SIO_000300: -2.471e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.02124183006536e-4
allele num: 9792
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 5
allele frequency: 7.502100588164687e-5
allele num: 66648
num of homozygotes: 0

Other
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allele count: 0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
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FS
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ClippingRankSum
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MQRankSum
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QD
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MQ
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DP
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SIO_000300: 2.225387e6

ReadPosRankSum
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BaseQRankSum
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SIO_000300: -2.341e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.021033285685113e-4
allele num: 9794
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66644
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.988e1

QD
type: SiteQuality
SIO_000300: 1.161e1

VQSLOD
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SIO_000300: 1.04e-1

FS
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BaseQRankSum
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MQRankSum
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SIO_000300: 1.64e0

ReadPosRankSum
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InbreedingCoeff
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SIO_000300: -1.0e-4

DP
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SIO_000300: 2.22481e6

ClippingRankSum
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SIO_000300: 8.129999999999999e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500555205426008e-5
allele num: 66642
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

QD
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MQRankSum
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BaseQRankSum
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VQSLOD
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DP
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FS
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ClippingRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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African
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East Asian
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allele num: 8620
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European (Finnish)
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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QD
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MQ
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MQRankSum
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FS
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BaseQRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 4.503287399801856e-5
allele num: 66618
num of homozygotes: 0

African
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South Asian
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Latino
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num of homozygotes: 0

Other
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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ReadPosRankSum
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MQ
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6612
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.50159168718842e-5
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num of homozygotes: 0

East Asian
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Latino
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allele frequency: 0.0e0
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South Asian
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Other
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InbreedingCoeff
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DP
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FS
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MQ
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QD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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Latino
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South Asian
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ClippingRankSum
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MQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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MQ
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.503216884132043e-5
allele num: 66524
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European (Finnish)
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num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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Other
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InbreedingCoeff
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BaseQRankSum
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QD
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FS
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ClippingRankSum
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66482
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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Latino
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allele frequency: 0.0e0
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MQ
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SIO_000300: 5.978e1

BaseQRankSum
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QD
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ClippingRankSum
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MQRankSum
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FS
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DP
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ReadPosRankSum
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SIO_000300: 1.92e0

VQSLOD
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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East Asian
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allele num: 8614
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European (Finnish)
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Other
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Latino
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African
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QD
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11570
num of homozygotes: 0

Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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African
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South Asian
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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DP
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MQRankSum
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MQ
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FS
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QD
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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Latino
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African
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Other
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European (Finnish)
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East Asian
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ReadPosRankSum
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BaseQRankSum
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DP
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MQRankSum
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FS
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ClippingRankSum
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VQSLOD
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QD
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MQ
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 68
bin: 4.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162520344106022e-4
allele num: 8602
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15358
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66274
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9782
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

DP
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SIO_000300: 2.219979e6

VQSLOD
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QD
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SIO_000300: 1.584e1

MQRankSum
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SIO_000300: -1.44e0

BaseQRankSum
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SIO_000300: -6.21e-1

ClippingRankSum
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SIO_000300: 2.49e-1

MQ
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SIO_000300: 5.791e1

FS
type: SiteQuality
SIO_000300: 2.616e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3490
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15342
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66256
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.593809441466367e-4
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.18e0

InbreedingCoeff
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SIO_000300: 4.0e-4

QD
type: SiteQuality
SIO_000300: 1.361e1

FS
type: SiteQuality
SIO_000300: 1.16e0

MQ
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SIO_000300: 5.897e1

DP
type: SiteQuality
SIO_000300: 2.219155e6

VQSLOD
type: SiteQuality
SIO_000300: 3.31e-1

ReadPosRankSum
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SIO_000300: -1.3e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.6e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8598
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509798592867711e-5
allele num: 66234
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15290
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.55e-1

ReadPosRankSum
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SIO_000300: 2.4e-2

BaseQRankSum
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SIO_000300: -1.489e0

ClippingRankSum
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SIO_000300: -1.56e-1

MQRankSum
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SIO_000300: 5.600000000000001e-1

InbreedingCoeff
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SIO_000300: 5.0e-4

DP
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SIO_000300: 2.216089e6

FS
type: SiteQuality
SIO_000300: 2.097e0

QD
type: SiteQuality
SIO_000300: 1.07e1

MQ
type: SiteQuality
SIO_000300: 5.986e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2222
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8586
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9768
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.023157385573493e-5
allele num: 66156
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15040
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 882
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.056e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.090000000000001e-1

MQRankSum
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SIO_000300: 3.06e-1

MQ
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SIO_000300: 5.958e1

QD
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SIO_000300: 1.578e1

ClippingRankSum
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SIO_000300: -1.633e0

BaseQRankSum
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SIO_000300: 3.33e0

DP
type: SiteQuality
SIO_000300: 2.204938e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4575
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variant carriers: 0

GenotypeQuality
all individuals: 4345
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66010
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 4.101722723543889e-4
allele num: 9752
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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MQ
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ReadPosRankSum
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9740
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14530
num of homozygotes: 0

European (Non-Finnish)
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allele count: 3
allele frequency: 4.546418937350347e-5
allele num: 65986
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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FS
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DP
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 5
allele frequency: 5.130309870716191e-4
allele num: 9746
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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FS
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DP
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InbreedingCoeff
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BaseQRankSum
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QD
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VQSLOD
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MQ
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519248883352071e-5
allele num: 65822
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
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SIO_000300: 5.97e1

InbreedingCoeff
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SIO_000300: 3.6e-3

MQRankSum
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SIO_000300: -2.05e-1

QD
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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SIO_000300: -1.258e0

DP
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SIO_000300: 2.189264e6

ClippingRankSum
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SIO_000300: 9.96e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 17871
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13008
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 402
num of homozygotes: 0

African
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allele count: 2
allele frequency: 6.430868167202572e-4
allele num: 3110
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

DP
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SIO_000300: 9.35921e5

QD
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ReadPosRankSum
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MQRankSum
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FS
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MQ
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SIO_000300: 5.988e1

ClippingRankSum
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SIO_000300: -2.63e-1

BaseQRankSum
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SIO_000300: 8.19e0

VQSLOD
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SIO_000300: 1.1e0

InbreedingCoeff
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SIO_000300: -3.61e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1927
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2044
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 452
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.11358574610245e-3
allele num: 898
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.138e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

BaseQRankSum
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SIO_000300: 1.11e0

DP
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SIO_000300: 9.7566e5

QD
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SIO_000300: 1.5e1

ClippingRankSum
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SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

FS
type: SiteQuality
SIO_000300: 5.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 303
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variant carriers: 166

GenotypeDepth
all individuals: 147
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variant carriers: 34

GenotypeDepth
all individuals: 100
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variant carriers: 8

GenotypeQuality
all individuals: 7564
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variant carriers: 3600

GenotypeQuality
all individuals: 2276
bin: 1.75e1
variant carriers: 226

GenotypeQuality
all individuals: 18069
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variant carriers: 162

GenotypeQuality
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variant carriers: 78

GenotypeQuality
all individuals: 2865
bin: 2.5e0
variant carriers: 4

GenotypeQuality
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variant carriers: 121

GenotypeQuality
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variant carriers: 81

GenotypeQuality
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GenotypeQuality
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variant carriers: 136

GenotypeQuality
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variant carriers: 232

GenotypeQuality
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bin: 3.25e1
variant carriers: 111

GenotypeQuality
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variant carriers: 37

GenotypeQuality
all individuals: 17081
bin: 2.25e1
variant carriers: 285

GenotypeQuality
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variant carriers: 81

GenotypeQuality
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bin: 1.25e1
variant carriers: 180

GenotypeQuality
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variant carriers: 128

GenotypeQuality
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GenotypeQuality
all individuals: 246
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variant carriers: 216

GenotypeQuality
all individuals: 823
bin: 6.75e1
variant carriers: 223

GenotypeQuality
all individuals: 1927
bin: 6.25e1
variant carriers: 241

African
type: Population
allele count: 181
allele frequency: 5.731475617479417e-2
allele num: 3158
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 47
allele frequency: 1.039823008849557e-1
allele num: 452
num of homozygotes: 1

Latino
type: Population
allele count: 80
allele frequency: 8.908685968819599e-2
allele num: 898
num of homozygotes: 2

East Asian
type: Population
allele count: 431
allele frequency: 2.108610567514677e-1
allele num: 2044
num of homozygotes: 33

Other
type: Population
allele count: 28
allele frequency: 1.15702479338843e-1
allele num: 242
num of homozygotes: 2

South Asian
type: Population
allele count: 1861
allele frequency: 2.193540782649694e-1
allele num: 8484
num of homozygotes: 208

European (Non-Finnish)
type: Population
allele count: 1219
allele frequency: 9.024281907018063e-2
allele num: 13508
num of homozygotes: 34

DP
type: SiteQuality
SIO_000300: 9.7566e5

FS
type: SiteQuality
SIO_000300: 5.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

BaseQRankSum
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SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.5e1

MQRankSum
type: SiteQuality
SIO_000300: 2.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.138e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

GenotypeDepth
all individuals: 421
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 4823
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 932
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 291
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GenotypeQuality
all individuals: 496
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3036
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 7.917656373713381e-5
allele num: 12630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1720
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8190
num of homozygotes: 0

VQSLOD
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SIO_000300: -1.944e0

MQRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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FS
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QD
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SIO_000300: 1.277e1

BaseQRankSum
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SIO_000300: 9.62e-1

DP
type: SiteQuality
SIO_000300: 9.16933e5

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4823
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variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12526
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 360
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3026
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
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Other
type: Population
allele count: 0
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allele num: 240
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.05e-2

QD
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MQRankSum
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VQSLOD
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MQ
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SIO_000300: 6.0e1

DP
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SIO_000300: 9.12267e5

BaseQRankSum
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SIO_000300: -1.3e0

FS
type: SiteQuality
SIO_000300: 3.136e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 132
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 36
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GenotypeQuality
all individuals: 495
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 40
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GenotypeQuality
all individuals: 26
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Latino
type: Population
allele count: 1
allele frequency: 1.2531328320802e-3
allele num: 798
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12354
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 344
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3004
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FS
type: SiteQuality
SIO_000300: 2.027e0

DP
type: SiteQuality
SIO_000300: 9.0764e5

ReadPosRankSum
type: SiteQuality
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MQRankSum
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ClippingRankSum
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SIO_000300: 0.0e0

MQ
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.17e-2

QD
type: SiteQuality
SIO_000300: 1.418e1

BaseQRankSum
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SIO_000300: 1.36e0

GenotypeDepth
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bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1376
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1890
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 397
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 218
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8078
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 268
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2816
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.93e-2

VQSLOD
type: SiteQuality
SIO_000300: -8.905e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

QD
type: SiteQuality
SIO_000300: 1.037e1

DP
type: SiteQuality
SIO_000300: 8.73726e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

GenotypeDepth
all individuals: 132
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 787
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1261
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 628
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 409
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4964
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24959
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4818
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10406
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7982
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1108
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.88e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.38e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.109999999999999e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 8.76e-1

DP
type: SiteQuality
SIO_000300: 8.42233e5

VQSLOD
type: SiteQuality
SIO_000300: -1.911e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3611
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1471
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1987
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11320
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.63929051506508e-5
allele num: 61002
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16212
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.02e1

MQRankSum
type: SiteQuality
SIO_000300: 9.98e-1

FS
type: SiteQuality
SIO_000300: 1.905e0

VQSLOD
type: SiteQuality
SIO_000300: 4.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.03e-2

DP
type: SiteQuality
SIO_000300: 1.779035e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.262e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 3596
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10058
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 268
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 187
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 3.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61012
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.519756838905775e-4
allele num: 6580
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11324
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 3.0e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.780854e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

MQ
type: SiteQuality
SIO_000300: 5.957e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.251e0

QD
type: SiteQuality
SIO_000300: 1.511e1

GenotypeQuality
all individuals: 4373
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3071
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1979
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6369
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 132
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.639935714519991e-5
allele num: 60978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -4.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.04e-1

QD
type: SiteQuality
SIO_000300: 1.086e1

FS
type: SiteQuality
SIO_000300: 1.981e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.945e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

DP
type: SiteQuality
SIO_000300: 1.782687e6

GenotypeQuality
all individuals: 521
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3561
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3058
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1973
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16210
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.49500998003992e-4
allele num: 8016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.86e0

VQSLOD
type: SiteQuality
SIO_000300: 4.24e-1

QD
type: SiteQuality
SIO_000300: 1.376e1

FS
type: SiteQuality
SIO_000300: 1.358e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.43e-1

DP
type: SiteQuality
SIO_000300: 1.783584e6

GenotypeQuality
all individuals: 115
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6361
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1460
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1975
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3567
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 3.740648379052369e-4
allele num: 8020
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61050
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.48e0

DP
type: SiteQuality
SIO_000300: 1.785889e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.77e-1

FS
type: SiteQuality
SIO_000300: 5.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.54e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.46e-1

QD
type: SiteQuality
SIO_000300: 1.43e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24698
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10105
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3557
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1977
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16212
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11324
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.636554071746531e-5
allele num: 61104
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.791036e6

QD
type: SiteQuality
SIO_000300: 1.296e1

VQSLOD
type: SiteQuality
SIO_000300: -7.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 7.536e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.944e0

MQRankSum
type: SiteQuality
SIO_000300: 2.61e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.999999999999999e-3

MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3562
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6357
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 91
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10130
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8042
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.635858007524947e-5
allele num: 61130
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 826
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.08e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.8e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.264e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.74e-1

DP
type: SiteQuality
SIO_000300: 1.791595e6

MQ
type: SiteQuality
SIO_000300: 5.894e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.28e0

QD
type: SiteQuality
SIO_000300: 1.239e1

GenotypeQuality
all individuals: 42
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10156
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3565
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25027
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8074
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.818342151675486e-5
allele num: 11340
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61188
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.88e-1

MQ
type: SiteQuality
SIO_000300: 5.869e1

VQSLOD
type: SiteQuality
SIO_000300: -1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.174e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.794955e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.68e-1

QD
type: SiteQuality
SIO_000300: 7.93e0

GenotypeQuality
all individuals: 611
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3058
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6360
bin: 9.75e1
variant carriers: 3

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.901320088877271e-5
allele num: 61208
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8090
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.3e-1

MQ
type: SiteQuality
SIO_000300: 5.926e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.66e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.644e0

FS
type: SiteQuality
SIO_000300: 7.209e0

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 1.168e1

DP
type: SiteQuality
SIO_000300: 1.796045e6

GenotypeQuality
all individuals: 618
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25108
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10174
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3060
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.267546725918181e-5
allele num: 61208
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8094
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.79e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.751e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

FS
type: SiteQuality
SIO_000300: 1.3012e1

DP
type: SiteQuality
SIO_000300: 1.79611e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.84e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.69e0

GenotypeQuality
all individuals: 3566
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4356
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10174
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25108
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.76273576590869e-4
allele num: 11346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61208
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16214
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.751e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.84e-1

DP
type: SiteQuality
SIO_000300: 1.79611e6

FS
type: SiteQuality
SIO_000300: 1.3012e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.69e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

GenotypeQuality
all individuals: 27
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 594
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3516
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1908
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 10099
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 12
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4278
bin: 7.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.800718719372754e-5
allele num: 61220
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.415458937198068e-3
allele num: 828
num of homozygotes: 0

African
type: Population
allele count: 1114
allele frequency: 1.372935666748829e-1
allele num: 8114
num of homozygotes: 79

South Asian
type: Population
allele count: 3
allele frequency: 1.850252867891945e-4
allele num: 16214
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.519295047098146e-4
allele num: 6582
num of homozygotes: 0

Latino
type: Population
allele count: 62
allele frequency: 5.46448087431694e-3
allele num: 11346
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.228e1

VQSLOD
type: SiteQuality
SIO_000300: 4.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.429999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.25e0

FS
type: SiteQuality
SIO_000300: 1.876e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.14e-1

DP
type: SiteQuality
SIO_000300: 1.849701e6

GenotypeQuality
all individuals: 128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3587
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4337
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.632226683641824e-5
allele num: 61266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e-2

MQ
type: SiteQuality
SIO_000300: 5.95e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: -1.398e0

DP
type: SiteQuality
SIO_000300: 1.79208e6

QD
type: SiteQuality
SIO_000300: 1.71e1

FS
type: SiteQuality
SIO_000300: 1.1513e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.32e-1

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25585
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3028
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3587
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.264240248082259e-5
allele num: 61270
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -9.17e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.66e-1

QD
type: SiteQuality
SIO_000300: 1.153e1

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

FS
type: SiteQuality
SIO_000300: 3.336e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.792271e6

GenotypeQuality
all individuals: 607
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4336
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1937
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3589
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5944
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.1667488899852e-5
allele num: 16216
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.865e0

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.099e0

DP
type: SiteQuality
SIO_000300: 1.792315e6

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

QD
type: SiteQuality
SIO_000300: 1.123e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3588
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3029
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.85002466699556e-4
allele num: 16216
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61270
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

DP
type: SiteQuality
SIO_000300: 1.792419e6

MQ
type: SiteQuality
SIO_000300: 5.982e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e0

QD
type: SiteQuality
SIO_000300: 1.106e1

FS
type: SiteQuality
SIO_000300: 7.59e0

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.034e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.66e-1

GenotypeQuality
all individuals: 4335
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1417
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10349
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25614
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1934
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61272
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.230920728705071e-4
allele num: 8124
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.66e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

MQRankSum
type: SiteQuality
SIO_000300: -1.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-2

FS
type: SiteQuality
SIO_000300: 5.718e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.171e0

QD
type: SiteQuality
SIO_000300: 1.336e1

DP
type: SiteQuality
SIO_000300: 1.79247e6

GenotypeQuality
all individuals: 3586
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3031
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1416
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25605
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.305610862682378e-4
allele num: 61274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.843e0

MQRankSum
type: SiteQuality
SIO_000300: 3.92e-1

QD
type: SiteQuality
SIO_000300: 1.064e1

MQ
type: SiteQuality
SIO_000300: 5.932e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.367e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-1

DP
type: SiteQuality
SIO_000300: 1.792853e6

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3586
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10350
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5943
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4332
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.632013578352972e-5
allele num: 61274
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.859e0

VQSLOD
type: SiteQuality
SIO_000300: 2.82e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.104e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.99e-1

FS
type: SiteQuality
SIO_000300: 2.214e0

QD
type: SiteQuality
SIO_000300: 1.098e1

DP
type: SiteQuality
SIO_000300: 1.792457e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3586
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3029
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10350
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.815232722143864e-5
allele num: 11344
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8200
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.649999999999999e-1

FS
type: SiteQuality
SIO_000300: 1.412e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.17e0

MQRankSum
type: SiteQuality
SIO_000300: -1.12e-1

DP
type: SiteQuality
SIO_000300: 1.792143e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.58e-1

QD
type: SiteQuality
SIO_000300: 1.665e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeQuality
all individuals: 59
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4328
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5942
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3029
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3580
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.632439844591727e-5
allele num: 61258
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11340
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8116
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2034e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.356e0

DP
type: SiteQuality
SIO_000300: 1.791505e6

MQ
type: SiteQuality
SIO_000300: 5.981e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

MQRankSum
type: SiteQuality
SIO_000300: 1.83e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.522e0

VQSLOD
type: SiteQuality
SIO_000300: -1.819e0

QD
type: SiteQuality
SIO_000300: 8.800000000000001e0

GenotypeQuality
all individuals: 1414
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1931
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4326
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3024
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.439619419370578e-4
allele num: 8198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61242
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8102
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.790158e6

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

QD
type: SiteQuality
SIO_000300: 1.545e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

GenotypeQuality
all individuals: 3024
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1931
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8102
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.306293066849548e-4
allele num: 61242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11332
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.21e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.53e-1

DP
type: SiteQuality
SIO_000300: 1.790158e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-1

QD
type: SiteQuality
SIO_000300: 1.545e1

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24194
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8020
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11322
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.277936211361327e-5
allele num: 61014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16206
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.08e-1

DP
type: SiteQuality
SIO_000300: 1.77135e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.94e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

QD
type: SiteQuality
SIO_000300: 1.458e1

GenotypeQuality
all individuals: 1921
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24194
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5928
bin: 9.75e1
variant carriers: 1

Latino
type: Population
allele count: 1
allele frequency: 8.832361773538245e-5
allele num: 11322
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8020
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16206
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.18e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

MQ
type: SiteQuality
SIO_000300: 5.945e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.458e1

DP
type: SiteQuality
SIO_000300: 1.77135e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.94e-1